Al Jarad N, Demertzis P, Jones D J, Barnes N C, Rudd R M, Gaya H, Wedzicha J A, Hughes D T, Empey D W
East London Tuberculosis Centre, London Chest Hospital, UK.
Thorax. 1996 Feb;51(2):137-9. doi: 10.1136/thx.51.2.137.
Patients with non-tuberculous mycobacteria are usually started on conventional antituberculous triple therapy once acid fast bacilli are detected, before the exact type of mycobacteria has been identified. The ability to identify the characteristics of patients with tuberculous and non-tuberculous mycobacteria may be helpful in identifying before treatment those patients more likely to have non-tuberculous infection.
A retrospective study was conducted of all patients in one unit in whom non-tuberculous mycobacteria were identified in sputum or bronchoalveolar washings in the period 1987-93. The pattern of drug resistance was determined from laboratory records, and all case notes and chest radiographs were reviewed to identify the underlying disease and treatment outcome. All cases were compared with a matched control group of patients with culture positive Mycobacterium tuberculosis diagnosed during the same period.
In the period studied there were 70 non-tuberculous and 221 tuberculous isolates. The non-tuberculous bacteria were typed as follows: M xenopi 23 (33%), M kansasii 19 (27%), M fortuitum 14 (20%), others 14 (20%). Of those with non-tuberculous mycobacteria, 83% were white subjects compared with 47% for tuberculosis. Patients with non-tuberculous mycobacteria were older than those with tuberculosis. Pre-existing lung disease or AIDS was present in 81% of patients with non-tuberculous mycobacteria and in 17% of patients with tuberculosis. Sensitivity to rifampicin and ethambutol was seen in 95% of M xenopi and 96% of M kansasii isolates. Relapse occurred in 60% of cases infected with M xenopi, 20% infected with M kansasii, and in 7% of cases with tuberculosis.
In the population studied non-tuberculous mycobacteria occurred most frequently in elderly white subjects with pre-existing lung disease. If mycobacteria are detected in this group, consideration should be given to the possibility of non-tuberculous infection before embarking on treatment. A combination containing rifampicin and ethambutol is effective. The relapse rate for infection with M xenopi is high and prospective studies of the effect of the above combination of antituberculosis drugs are needed.
一旦检测到抗酸杆菌,在未明确分枝杆菌的确切类型之前,非结核分枝杆菌患者通常会开始接受传统的抗结核三联疗法。识别结核分枝杆菌和非结核分枝杆菌患者的特征,可能有助于在治疗前确定那些更可能患有非结核感染的患者。
对1987 - 1993年期间在一个科室痰液或支气管肺泡灌洗物中鉴定出非结核分枝杆菌的所有患者进行回顾性研究。从实验室记录中确定耐药模式,并查阅所有病历和胸部X光片以确定基础疾病和治疗结果。将所有病例与同期诊断为结核分枝杆菌培养阳性的匹配对照组患者进行比较。
在研究期间,有70株非结核分枝杆菌和221株结核分枝杆菌分离株。非结核分枝杆菌类型如下:偶发分枝杆菌23株(33%),堪萨斯分枝杆菌19株(27%),偶然分枝杆菌14株(20%),其他14株(20%)。在非结核分枝杆菌患者中,83%为白人,而结核病患者中这一比例为47%。非结核分枝杆菌患者比结核病患者年龄更大。81%的非结核分枝杆菌患者和17%的结核病患者存在既往肺部疾病或艾滋病。95%的偶发分枝杆菌分离株和96%的堪萨斯分枝杆菌分离株对利福平和乙胺丁醇敏感。偶发分枝杆菌感染病例的复发率为60%,堪萨斯分枝杆菌感染病例为20%,结核病病例为7%。
在所研究的人群中,非结核分枝杆菌最常见于患有既往肺部疾病的老年白人。如果在该组中检测到分枝杆菌,在开始治疗前应考虑非结核感染的可能性。含利福平和乙胺丁醇的联合用药有效。偶发分枝杆菌感染的复发率很高,需要对上述抗结核药物联合治疗的效果进行前瞻性研究。